Gene >> SHCBP1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303383 |
| Start |
46581943:46581943(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1805C>T |
| AA Mutation |
p.Thr602Ile(p.T602I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303383 |
| Start |
46583533:46583533(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1676C>G |
| AA Mutation |
p.Ala559Gly(p.A559G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |